Roshan B Colah: search on Z-Library

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1

A single mutation is responsible for the high prevalence of G6pD deficiency in the Vataliya Prajapatis—An endogamous caste group from Western India

Sridevi Sukumar, Roshan B. Colah, Dipika Mohanty, Sanmukh R. Joshi

Journal:

American Journal of Hematology

Year:

2001

Language:

english

File:

PDF, 441 KB

english, 2001

2

Burden of thalassemia in India: The road map for control

Colah, Roshan, Italia, Khushnooma, Gorakshakar, Ajit

Journal:

Pediatric Hematology Oncology Journal

Year:

2017

Language:

english

File:

PDF, 713 KB

english, 2017

3

Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India

Rati Chalvam, Roshan B. Colah, Dipika Mohanty, Kanjaksha Ghosh, Malay B. Mukherjee

Journal:

Blood Cells, Molecules, and Diseases

Year:

2009

Language:

english

File:

PDF, 113 KB

english, 2009

4

Molecular Characterization of δβ-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in the Indian Population

Nadkarni, Anita, Wadia, Marukh, Gorakshakar, Ajit, Kiyama, Ryoiti, Colah, Roshan B., Mohanty, Dipika

Journal:

Year:

2008

Language:

english

File:

PDF, 207 KB

english, 2008

5

Production of Murine Monoclonal Antibody to Fetal Hemoglobin

Iyer, Yegneshwar S., Patwardhan, Manisha, Pujari, Vaishali, Shinde, Gayatri, Keertikar, Paritosh, Kulkarni, Swati, Colah, Roshan B., Mohanty, Dipika

Journal:

Year:

2003

Language:

english

File:

PDF, 93 KB

english, 2003

6

Assessing the impact of screening and counselling high school children for β-thalassaemia in India

Colah, Roshan, Thomas, Mariamma, Mayekar, Pramod

Journal:

Journal of Medical Screening

Year:

2007

Language:

english

File:

PDF, 38 KB

english, 2007

7

Can hydroxyurea serve as a free radical scavenger and reduce iron overload in β-thalassemia patients?

Italia, Khushnooma, Chandrakala, S., Ghosh, Kanjaksha, Colah, Roshan

Journal:

Free Radical Research

Year:

2016

Language:

english

File:

PDF, 694 KB

english, 2016

8

Red cell distribution width and its association with mortality in neonatal sepsis

Martin, Snehal L., Desai, Saumil, Nanavati, Ruchi, Colah, Roshan B., Ghosh, Kanjaksha, Mukherjee, Malay B.

Journal:

Journal of Maternal-Fetal and Neonatal Medicine

Year:

2018

Language:

english

File:

PDF, 860 KB

english, 2018

9

The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center

Nadkarni, Anita H., Gorakshakar, Ajit C., Sawant, Pratibha M., Italia, Khushnooma Y., Upadhye, Dipti S., Gorivale, Manju S., Mehta, Pallavi R., Hariharan, Priya, Ghosh, Kanjaksha, Colah, Roshan B.

Journal:

International Journal of Laboratory Hematology (Blackwell)

Year:

2018

Language:

english

File:

PDF, 881 KB

english, 2018

10

Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders

Hariharan, Priya, Colah, Roshan, Ghosh, Kanjaksha, Nadkarni, Anita

Journal:

Year:

2018

Language:

english

File:

PDF, 864 KB

english, 2018

11

Factor VIII and IX gene polymorphisms and carrier analysis in Indian population

Shetty, Shrimati, Ghosh, Kanjaksha, Pathare, Anil, Colah, Roshan, Badakare, Suresh, Mohanty, Dipika

Journal:

American Journal of Hematology

Year:

1997

Language:

english

File:

PDF, 636 KB

english, 1997

12

Effect of α-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in India

Mukherjee, Malay B., Lu, Chang Yong, Ducrocq, Rolande, Gangakhedkar, Raman R., Colah, Roshan B., Kadam, Megha D., Mohanty, Dipika, Nagel, Ronald L., Krishnamoorthy, Rajagopal

Journal:

American Journal of Hematology

Year:

1997

Language:

english

File:

PDF, 138 KB

english, 1997

13

Alpha Genotyping in a Heterogeneous Indian Population

Anita H. Nadkarni, Ajit C. Gorakshakar, Dipika Mohanty, Roshan B. Colah

Journal:

American Journal of Hematology

Year:

1996

Language:

english

File:

PDF, 162 KB

english, 1996

14

β-Thalassemia gene flow from India to Mauritius

Ajit C. Gorakshakar, Kanjaksha Ghosh, Roshan B. Colah, Dipika Mohanty

Journal:

American Journal of Hematology

Year:

2000

Language:

english

File:

PDF, 156 KB

english, 2000

15

Symptomatic presentation of a sickle cell heterozygote: An evaluation of genetic factors

Malay B. Mukherjee, Reema R. Surve, Ajit C. Gorakshakar, Raman R. Gangakhedkar, Roshan B. Colah, Dipika Mohanty

Journal:

American Journal of Hematology

Year:

2001

Language:

english

File:

PDF, 1.80 MB

english, 2001

16

Molecular pathogenesis and clinical variability of β-thalassemia syndromes among Indians

Anita Nadkarni, A.C. Gorakshakar, C.Y. Lu, R. Krishnamoorthy, K. Ghosh, Roshan Colah, Dipika Mohanty

Journal:

American Journal of Hematology

Year:

2001

Language:

english

File:

PDF, 44 KB

english, 2001

17

Congenital methemoglobinemia caused by Hb-MRatnagiri (β-63CAT→TAT, His→Tyr) in an Indian family

Prabhakar S. Kedar, Anita H. Nadkarni, Supriya Phanasgoankar, Manisha Madkaikar, Kanjaksha Ghosh, Ajit C. Gorakshakar, Roshan B. Colah, Dipika Mohanty

Journal:

American Journal of Hematology

Year:

2005

Language:

english

File:

PDF, 68 KB

english, 2005

18

Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D

Boris E. Shmukler, Prabhakar S. Kedar, Prashant Warang, Mukesh Desai, Manisha Madkaikar, Kanjaksha Ghosh, Roshan B. Colah, Seth L. Alper

Journal:

American Journal of Hematology

Year:

2010

Language:

english

File:

PDF, 1.04 MB

english, 2010

19

Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH-cytochrome b5 reductase gene mutations

Prabhakar S. Kedar, Prashant Warang, Kanjaksha Ghosh, Roshan B. Colah

Journal:

American Journal of Hematology

Year:

2011

Language:

english

File:

PDF, 150 KB

english, 2011

20

A comparison of the choice of monoclonal antibodies for recovery of fetal cells from maternal blood using FACS for noninvasive prenatal diagnosis of hemoglobinopathies

Edna D'Souza, Kanjaksha Ghosh, Roshan Colah

Journal:

Cytometry Part B: Clinical Cytometry

Year:

2009

Language:

english

File:

PDF, 155 KB

english, 2009

21

Flow cytometric osmotic fragility—An effective screening approach for red cell membranopathies

Prashant Warang, Maya Gupta, Prabhakar Kedar, Kanjaksha Ghosh, Roshan Colah

Journal:

Cytometry Part B: Clinical Cytometry

Year:

2011

Language:

english

File:

PDF, 679 KB

english, 2011

22

The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies

Khushnooma Y. Italia, Farah F. Jijina, Dipty Jain, Rashid Merchant, Anita H. Nadkarni, Malay Mukherjee, Kanjaksha Ghosh, Roshan B. Colah

Journal:

Clinical Biochemistry

Year:

2010

Language:

english

File:

PDF, 188 KB

english, 2010

23

Proteomic investigation on the pyk-F gene knockout Escherichia coli for aromatic amino acid production

Prabhakar Kedar, Roshan Colah, Kazuyuki Shimizu

Journal:

Enzyme and Microbial Technology

Year:

2007

Language:

english

File:

PDF, 1.07 MB

english, 2007

24

G6PD gene mutations in India producing drug-induced haemolytic anaemia

Sridevi Sukumar, Roshan Colah, Dipika Mohanty

Journal:

British Journal of Haematology

Year:

2002

Language:

english

File:

PDF, 40 KB

english, 2002

25

Prenatal diagnosis of sickle syndromes in India: dilemmas in counselling

Roshan Colah, Reema Surve, Anita Nadkarni, Ajit Gorakshakar, Supriya Phanasgaonkar, Poornima Satoskar, Dipika Mohanty

Journal:

Prenatal Diagnosis

Year:

2005

Language:

english

File:

PDF, 94 KB

english, 2005

26

Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family

Neerja Gupta, Paola Bianchi, Elisa Fermo, Madhulika Kabra, Prashant Warang, Prabhakar Kedar, Nomeeta Gupta, Roshan Colah

Journal:

Prenatal Diagnosis

Year:

2007

Language:

english

File:

PDF, 86 KB

english, 2007

27

Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of β-thalassemia

Mahrukh R. Wadia, Supriya P. Phanasgaokar, Anita H. Nadkarni, Reema R. Surve, Ajit C. Gorakshakar, Roshan B. Colah, Dipika Mohanty

Journal:

Prenatal Diagnosis

Year:

2002

Language:

english

File:

PDF, 199 KB

english, 2002

28

Masking of the clinical severity of severe haemophilia A in a patient with β-thalassemia major—its implications in prenatal diagnosis

Roshan Colah, Shrimati Shetty, Anita Nadkarni, Kanjaksha Ghosh, Dipika Mohanty

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 97 KB

english, 2004

29

Glucose–6–phosphate dehydrogenase deficiency in India

Dipika Mohanty, Malay B. Mukherjee, Roshan B. Colah

Journal:

Indian Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 512 KB

english, 2004

30

Red cell pyruvate kinase deficiency in neonatal jaundice cases in India

Prabhakar S. Kedar, Prashant Warang, Roshan B. Colah, Dipika Mohanty

Journal:

Indian Journal of Pediatrics

Year:

2006

Language:

english

File:

PDF, 346 KB

english, 2006

31

β-Thalassemias : Expression, molecular mechanisms and mutations in Indians

Roshan Colah, Dipika Mohanty

Journal:

Indian Journal of Pediatrics

Year:

1998

Language:

english

File:

PDF, 644 KB

english, 1998

32

Origin of the codon 47 (+A) β-thalassaemia mutation among the Nicobarese of the Andaman and Nicobar islands in India

Ajit C. Gorakshakar, Manoj K. Das, Supriya P. Phanasgaokar, Anita H. Nadkarni, Roshan B. Colah, Dipika Mohanty

Journal:

British Journal of Haematology

Year:

2007

Language:

english

File:

PDF, 52 KB

english, 2007

33

Epidemiology of β-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat

Roshan Colah, Ajit Gorakshakar, Supriya Phanasgaonkar, Edna D’Souza, Anita Nadkarni, Reema Surve, Pratibha Sawant, Dilip Master, Ramesh Patel, Kanjaksha Ghosh, Dipika Mohanty

Journal:

British Journal of Haematology

Year:

2010

Language:

english

File:

PDF, 98 KB

english, 2010

34

Molecular Characterization of FUT1(H) Gene in the Bombay Phenotypes Detected in India

K Vasantha, Ajit Gorakshakar, Roshan Colah, Swati Kulkarni, Dipika Mohanty

Journal:

Transfusion Medicine

Year:

2005

Language:

english

File:

PDF, 195 KB

english, 2005

35

Molecular Characterization of Partial D Variants in India

Swati Kulkarni, Roshan Colah, Ajit Gorakshakar, Snehalata Gupte, Dipika Mohanty

Journal:

Transfusion Medicine

Year:

2005

Language:

english

File:

PDF, 195 KB

english, 2005

36

A Genome-Wide Search for Non-UGT1A1 Markers Associated with Unconjugated Bilirubin Level Reveals Significant Association with a Polymorphic Marker Near a Gene of the Nucleoporin Family

Shalini Datta, Abhijit Chowdhury, Malay Ghosh, Kaushik Das, Pankaj Jha, Roshan Colah, Mitali Mukerji, Partha P. Majumder

Journal:

Annals of Human Genetics

Year:

2012

Language:

english

File:

PDF, 566 KB

english, 2012

37

Prenatal diagnosis of HbE-Lepore and Hb Lepore-β-thalassemia: the importance of accurate genotyping of the couple at risk

Khushnooma Italia, Jayesh Sheth, Pratibha Sawant, Anita Nadkarni, Kanjaksha Ghosh, Roshan Colah

Journal:

Prenatal Diagnosis

Year:

2012

Language:

english

File:

PDF, 124 KB

english, 2012

38

Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population

Khushnooma Italia, Pratibha Sawant, Reema Surve, Marukh Wadia, Anita Nadkarni, Kanjaksha Ghosh, Roshan Colah

Journal:

European Journal of Haematology

Year:

2012

Language:

english

File:

PDF, 139 KB

english, 2012

39

Impact of β globin gene mutations on the clinical phenotype of β thalassemia in India

Roshan Colah, Anita Nadkarni, Ajit Gorakshakar, Supriya Phanasgaonkar, Reema Surve, P.G. Subramaniam, Nagnath Bondge, Kamala Pujari, Kanjaksha Ghosh, Dipika Mohanty

Journal:

Blood Cells, Molecules, and Diseases

Year:

2004

Language:

english

File:

PDF, 95 KB

english, 2004

40

Molecular basis of G6PD deficiency in India

Sridevi Sukumar, Malay B. Mukherjee, Roshan B. Colah, Dipika Mohanty

Journal:

Blood Cells, Molecules, and Diseases

Year:

2004

Language:

english

File:

PDF, 93 KB

english, 2004

41

Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G→A mutation

Sridevi Sukumar, Malay B. Mukherjee, Roshan B. Colah, Dipika Mohanty

Journal:

Blood Cells, Molecules, and Diseases

Year:

2005

Language:

english

File:

PDF, 72 KB

english, 2005

42

A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia

Prabhakar S. Kedar, Prashant Warang, Anita H. Nadkarni, Roshan B. Colah, Kanjaksha Ghosh

Journal:

Blood Cells, Molecules, and Diseases

Year:

2008

Language:

english

File:

PDF, 663 KB

english, 2008

43

Hydroxyurea in sickle cell disease—A study of clinico-pharmacological efficacy in the Indian haplotype

Khushnooma Italia, Dipty Jain, Sushma Gattani, Farah Jijina, Anita Nadkarni, Pratibha Sawant, Sona Nair, Dipika Mohanty, Kanjaksha Ghosh, Roshan Colah

Journal:

Blood Cells, Molecules, and Diseases

Year:

2009

Language:

english

File:

PDF, 549 KB

english, 2009

44

Response to hydroxyurea in β thalassemia major and intermedia: Experience in western India

Khushnooma Y. Italia, Farah J. Jijina, Rashid Merchant, Sangeeta Panjwani, Anita H. Nadkarni, Pratibha M. Sawant, Sona B. Nair, Kanjaksha Ghosh, Roshan B. Colah

Journal:

Clinica Chimica Acta

Year:

2009

Language:

english

File:

PDF, 226 KB

english, 2009

45

Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases

Stacy Colaco, Roshan Colah, K. Ghosh, Anita Nadkarni

Journal:

Clinica Chimica Acta

Year:

2012

Language:

english

File:

PDF, 306 KB

english, 2012

46

Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual case

Prabhakar S Kedar, Roshan B Colah, Kanjaksha Ghosh, Dipika Mohanty

Journal:

Clinica Chimica Acta

Year:

2004

Language:

english

File:

PDF, 116 KB

english, 2004

47

Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population

Roshan Colah, Ajit Gorakshakar, Anita Nadkarni, Supriya Phanasgaonkar, Reema Surve, Pratibha Sawant, Dipika Mohanty, Kanjaksha Ghosh

Journal:

Blood Cells, Molecules, and Diseases

Year:

2009

Language:

english

File:

PDF, 507 KB

english, 2009

48

UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults

Selma D'Silva, Roshan B. Colah, Kanjaksha Ghosh, Malay B. Mukherjee

Journal:

Year:

2013

Language:

english

File:

PDF, 171 KB

english, 2013

49

Carrier Screening for β-Thalassemia during Pregnancy in India: A 7-Year Evaluation

Colah, Roshan, Surve, Reema, Wadia, Marukh, Solanki, Prakash, Mayekar, Pramod, Thomas, Mariamma, Gorakshakar, Ajit, Dastur, Adi, Mohanty, Dipika

Journal:

Genetic Testing

Year:

2008

Language:

english

File:

PDF, 203 KB

english, 2008

50

Effect of a group of genetic markers around the 5′ regulatory regions of the β globin gene cluster linked to high HbF on the clinical severity of β thalassemia

Dabke, Pooja, Colah, Roshan B., Ghosh, K., Nadkarni, Anita

Journal:

Blood Cells, Molecules, and Diseases

Year:

2013

Language:

english

File:

PDF, 242 KB

english, 2013

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